Orcanos - Integrated Risk Management System
The Orcanos Risk Management tool essentially connects two different modules within the compliance process: Design Control (ALM) and Quality Management. The key to effective Risk Management is to reduce the level of risk that can impact an organization. More often that not, this relies heavily on knowing when a potential problem is about to happen. Orcanos’ Risk Management system has an integrated alert mechanism that notifies end users and stakeholders about any anomalies in the compliance process, generating a breakdown of impact analysis and actionable insights.
- Product complaints that have an associated risk, without any defined risk at that moment
- Risk without mitigation
- Test cases connected to risk mitigations that failed and which generated a level of risk
Compliance with ISO 14971:2019 requires medical device manufacturers to not only take a proactive attitude to risk management but also understand the perceived risks attached to the medical device itself. The concept of risk has two components; the probability of occurrence of harm and the consequences of that harm, both of which have varying degrees of severity.
Orcanos Risk Management has been designed to guide medical device manufacturers along the right path to compliance in a single workflow. Risk management is an accepted part of any product lifecycle, but the identification, tracking and mitigation of potential risks can become lost in paper-based and disparate systems.
Our system brings design control, risk and quality management into one integrated solution. By combining all the necessary elements for ISO 14971:2019 compliance into a centralized location, medical device manufacturers can reduce the risk of failure, ensure potential hazards are mitigated and prevent the occurence or consequences of harm.
Generating a digital Risk Management File that is compliant with regulatory standards can be done with a single clickRisk Automation
Automate the entire risk management system, such as Risk Level calculation method, automatic setup of probability based on the Hazardous situation, and more.
Define PFMEA, UFMEA, DFMEA easily, setup different calculations and different methodology based on the FMEA type
Setup the risk electronic form easily, define mandatory rules and access control, workflow for sign off and layout
Our automated and cloud-based solution is available to access anywhere and at any time, a Compliance Hub of your organizationEasy Setup
Configuration of your Risk Management processes can be completed in minutes.
- Fields layout
- Mandatory rules
- Risk Level Calculation
- Workflows and Sign-off
The Orcanos Risk Management tool can be customized to identify and highlight applicable risk elements in a medical device. This customization includes but is not limited to:
- Acceptable and desirable levels of risk within each product/component
- RPN (Criticality) Calculation
- Naming risk elements, such as who is affected and the mitigation type
- Setting up of multiple risk categories according to ISO 14971:2019
Companies can integrate the definition and implementation of risk mitigation plans. For example, the tool can help define which control elements are required for a specific risk, such as design artifacts.
Test cases can be tracked and traced to ensure that the level of risk has been properly assessed and verified, with these results saved for potential verification evidence
Integrate risk into your development, and to your QMS, to assure full traceability, and save 30% of the resources spent on manual management.
Orcanos Risk Management software includes a risk-based dashboard and access to analytic reports that can define a risk threshold.These embedded features can not only help trigger risk alerts and reports, but also increase team awareness of a product issue.
In addition, the in-built Document Generation tool will generate an RMF document ensuring automatic traceability that eliminates human error. This document can then be uploaded into the Orcanos e-DMS system for approval and e-signature.